Evidence map›Paper›PMID 38548340›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2024

Cone-Opponent Ganglion Cells in the Primate Fovea Tuned to Noncardinal Color Directions.

Tyler Godat, Kendall Kohout, Keith Parkins, Qiang Yang, Juliette E McGregor, William H Merigan, David R Williams, Sara S Patterson

Open access · greenAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.1field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Approaching a connectome of the human foveal retina.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Tyler GodatCenter for Visual Science, University of Rochester, Rochester, New York 14607.
Kendall KohoutCenter for Visual Science, University of Rochester, Rochester, New York 14607.
Keith ParkinsCenter for Visual Science, University of Rochester, Rochester, New York 14607.
Qiang YangCenter for Visual Science, University of Rochester, Rochester, New York 14607.
Juliette E McGregorCenter for Visual Science, University of Rochester, Rochester, New York 14607.
William H MeriganCenter for Visual Science, University of Rochester, Rochester, New York 14607.
David R WilliamsCenter for Visual Science, University of Rochester, Rochester, New York 14607.
Sara S PattersonCenter for Visual Science, University of Rochester, Rochester, New York 14607 spatte16@ur.rochester.edu.ORCID 0000-0003-4574-3935
University of Rochester · USCenter for Visual Communication (United States) · US

Funding

VISUAL SCIENCE RESEARCH CTR SUPPORTP30EY001319 · NEI · UNIVERSITY OF ROCHESTER · PI MICHELE RUCCI · 1985 to 2026
$17.5M
Physiological and perceptual examination of vision restoration R01EY021166 · NEI · UNIVERSITY OF ROCHESTER · PI MERIGAN, WILLIAM H · 2011 to 2023
$8.4M
VISUAL SCIENCET32EY007125 · NEI · UNIVERSITY OF ROCHESTER · PI Krystel R Huxlin, Duje Tadin · 1990 to 2026
$7.1M
High Resolution Mapping of Foveal Ganglion Cell Receptive Fields in the Living Primate EyeR01EY031467 · NEI · UNIVERSITY OF ROCHESTER · PI DAVID R WILLIAMS · 2021 to 2026
$3.5M
Linking rare primate ganglion cells to downstream visual functionsR00EY035323 · NEI · UNIVERSITY OF ROCHESTER · PI Sara S Patterson · 2024 to 2026
$750k
Linking rare primate ganglion cells to downstream visual functionsK99EY035323 · NEI · UNIVERSITY OF ROCHESTER · PI PATTERSON, SARA S · 2023 to 2024
$155k
Foveal ganglion cell function in the living eyeF32EY032318 · NEI · UNIVERSITY OF ROCHESTER · PI PATTERSON, SARA S · 2021 to 2022
$153k
NEI NIH HHS F32 EY032318NEI NIH HHS K99 EY035323NEI NIH HHS P30 EY001319NEI NIH HHS R00 EY035323NEI NIH HHS R01 EY021166NEI NIH HHS R01 EY031467NEI NIH HHS T32 EY007125
6 · The paper itself

Abstract

A long-standing question in vision science is how the three cone photoreceptor types-long (L), medium (M), and short (S) wavelength sensitive-combine to generate our perception of color. Hue perception can be described along two opponent axes: red-green and blue-yellow. Psychophysical measurements of color appearance indicate that the cone inputs to the red-green and blue-yellow opponent axes are M vs. L + S and L vs. M + S, respectively. However, the "cardinal directions of color space" revealed by psychophysical measurements of color detection thresholds following adaptation are L vs. M and S vs. L + M. These cardinal directions match the most common cone-opponent retinal ganglion cells (RGCs) in the primate retina. Accordingly, the cone opponency necessary for color appearance is thought to be established in the cortex. While neurons with the appropriate M vs. L + S and L vs. M + S opponency have been reported in the retina and lateral geniculate nucleus, their existence continues to be debated. Resolving this long-standing debate is necessary because a complete account of the cone opponency in the retinal output is critical for understanding how downstream neural circuits process color. Here, we performed adaptive optics calcium imaging to noninvasively measure foveal RGC light responses in the living

Indexed as

Color PerceptionFovea CentralisRetinal Cone Photoreceptor CellsRetinal Ganglion CellsAnimalsFemaleMacaca fascicularisMalePhotic Stimulationadaptive opticscolor visioncone opponencyfunctional imagingretinaretinal ganglion cell

Identifiers

PMID38548340
PMCPMC11063829
OpenAlexW4393253960

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.